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Potentiometric detection of the metabolic activity of human tumor cells

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Monitoring of cellular viability is a key part of toxicological assays in vitro. On-line monitoring of metabolic activity would be particularly useful for evaluation of responses to potential therapeutic compounds. Current assays are mostly based on fluorescent dyes and optical detection methods. These methods offer high sensitivity and specificity, however are not suitable for long-term on-line observations. Electrochemical methods can be an alternative for current protocols. Electrochemical detection is low cost and label-free, therefore suitable for long-term cell culture monitoring. In this work investigations on human cancer cells viability will be presented. Cells were cultured as two-dimensional monolayer or three-dimensional spheroids. Different cell culture media were examined. Potentiometric detection was used for continuous monitoring of cell culture as well as end-point investigations. Different growth phases were identified using applied method. Finally, response to an anticancer drug was successfully observed.
Rocznik
Strony
41--46
Opis fizyczny
Bibliogr. 30 poz., rys., wykr.
Twórcy
  • Department of Microbioanalytics, Institute of Biotechnology, Warsaw University of Technology
autor
autor
autor
autor
Bibliografia
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  • [4] Lin, R., and H. Chang. “Recent advances in three-dimensional multicellular spheroid culture for biomedical research.” Biotechnology Journal 3 (2008): 1172–1184.
  • [5] Sutherland, R. “Cell and Environmet Interactions in Tumor Microregions: The Multicell Spheroid Model.” Science 240 (1988): 177–184.
  • [6] Kim, J. “Three-dimensional tissue culture models in cancer biology”. Seminars in Cancer Biology 15 (2005): 365–377.
  • [7] Fischbach, C., et al. “Engineering tumors with 3D scaffolds.” Nature Methods 4 (2007): 855–860.
  • [8] Pampaloni, F., E. Stelzer, and A. Masoti. “Three-Dimensional Tissue Models for Drug Discovery and Toxicology.” Recent Patents on Biotechnology 3 (2009): 103–117.
  • [9] Ziółkowska, K., et al. “Lab-on-a-chip for cell engineering: towards cellular models mimicking in vivo.” Challenges of Modern Technology, 1(2), 2011: 79–82.
  • [10] Kelm, J., et al. “Method for Generation of Homogenous Multicellular Tumor Spheroid Applicable to a Wide Variety of Cell Types.” Biotechnology and Bioengineering 83 (2003): 173–180.
  • [11] Torisawa, Y., et al. “A multicellular spheroid array to realize spheroid formation, culture, and viability assay on a chip.” Biomaterials 28 (2007): 559–566.
  • [12] Friedrich, J., R. Ebner, and L. Kunz-Schughart. “Experimental anti-tumor therapy in 3-D: Spheroids—old hat or new challenge?”. International Journal of Radiation Biology 83 (2007): 849–871.
  • [13] Pampaloni, F., and E. Stelzer. “Three-Dimensional Cell Cultures in Toxicology”. Biotechnology and Genetic Engineering Reviews 26 (2009): 129–150.
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  • [18] Sivaraman, A., et al. “A Microscale In Vitro Physiological Model of the Liver: PredicitiveScreens for Drug Metabolism and Enzyme Induction”. Current Drug Metabolism 6 (2005): 569–591.
  • [19] Ziółkowska, K., et al. “Long-term three-dimensional cell culture and anticancer drug activity evaluation in a microfluidic chip”. Biosensors and Bioelectronics 40 (2013): 68–74.
  • [20] Ziółkowska, K., et al. „Development of a three-dimensional microfluidic system for long term tumor spheroid culture”. Sensors and Actuators B 173 (2012): 908–913.
  • [21] Ziółkowska, K., et al. “Novel designs and technologies for cell engineering”. Challenges of Modern Technology 2 (2011): 54–60.
  • [22] Ziółkowska, K., et al. “PDMS/Glass microfluidic cell culture system for cytotoxicity tests and cells passage.” Sensors and Actuators B 145 (2010): 533–542.
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  • [24] Hsiao, A., et al. “Microfluidic system for formation of PC-3 prostate cancer co-culture spheroids”. Biomaterials 30 (2009): 3020–3027.
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  • [30] Ziółkowska, K., et al. “Multiwell plate reader-compatible microfluidic system for long-term multicellular spheroid culture and monitoring”. Proceedings of the 16th International Conference on Miniaturized Systems for Chemistry and Life Sciences “MicroTAS 2012”. 2012: 407–409.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-07816bf4-67f9-47e8-b27c-3df5dbb73e62
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